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Analyses of the TCR repertoire of MHC class II-restricted innate CD4+ T cells
Experimental & Molecular Medicine ; : e154-2015.
Article in English | WPRIM | ID: wpr-190706
ABSTRACT
Analysis of the T-cell receptor (TCR) repertoire of innate CD4+ T cells selected by major histocompatibility complex (MHC) class II-dependent thymocyte-thymocyte (T-T) interaction (T-T CD4+ T cells) is essential for predicting the characteristics of the antigens that bind to these T cells and for distinguishing T-T CD4+ T cells from other types of innate T cells. Using the TCRmini Tg mouse model, we show that the repertoire of TCRalpha chains in T-T CD4+ T cells was extremely diverse, in contrast to the repertoires previously described for other types of innate T cells. The TCRalpha chain sequences significantly overlapped between T-T CD4+ T cells and conventional CD4+ T cells in the thymus and spleen. However, the diversity of the TCRalpha repertoire of T-T CD4+ T cells seemed to be restricted compared with that of conventional CD4+ T cells. Interestingly, the frequency of the parental OT-II TCRalpha chains was significantly reduced in the process of T-T interaction. This diverse and shifted repertoire in T-T CD4+ T cells has biological relevance in terms of defense against diverse pathogens and a possible regulatory role during peripheral T-T interaction.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Peptide Fragments / Phenotype / Spleen / Mice, Transgenic / Receptors, Antigen, T-Cell / CD4-Positive T-Lymphocytes / Histocompatibility Antigens Class II / Cell Communication / Cell Differentiation / Immunophenotyping Type of study: Prognostic study Limits: Animals Language: English Journal: Experimental & Molecular Medicine Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Peptide Fragments / Phenotype / Spleen / Mice, Transgenic / Receptors, Antigen, T-Cell / CD4-Positive T-Lymphocytes / Histocompatibility Antigens Class II / Cell Communication / Cell Differentiation / Immunophenotyping Type of study: Prognostic study Limits: Animals Language: English Journal: Experimental & Molecular Medicine Year: 2015 Type: Article